rs56393026

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs56393026(A;A)

Make rs56393026(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

4

Position

6302398

Gene	LOC107986257, WFS1

is a	snp
is	mentioned by
dbSNP	rs56393026
dbSNP (classic)	rs56393026
ClinGen	rs56393026
ebi	rs56393026
HLI	rs56393026
Exac	rs56393026
Gnomad	rs56393026
Varsome	rs56393026
LitVar	rs56393026
Map	rs56393026
PheGenI	rs56393026
Biobank	rs56393026
1000 genomes	rs56393026
hgdp	rs56393026
ensembl	rs56393026
geneview	rs56393026
scholar	rs56393026
google	rs56393026
pharmgkb	rs56393026
gwascentral	rs56393026
openSNP	rs56393026
23andMe	rs56393026
SNPshot	rs56393026
SNPdbe	rs56393026
MSV3d	rs56393026
GWAS Ctlg	rs56393026

Max Magnitude

0

ClinVar
Risk	rs56393026(A;A) rs56393026(C;C)
Alt	rs56393026(A;A) rs56393026(C;C)
Reference	Rs56393026(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	WFS1
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.6304125G>A
CLNSRC
CLNACC	RCV000199675.1,